gudid
Primary ID: CC118360
Platelet CHECK (UDI CC118360)
Manufactured by SYSMEX CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Platelet CHECK - Primary ID CC118360
Device Regulatory Overview
The Platelet CHECK (Model/Catalog Number: CC118360) is a medical device manufactured by SYSMEX CORPORATION. This product is indexed under FDA Product Code / Category Classification GJP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CC118360
- Product Code / EMDN
- GJP
- Device Name
- Platelet CHECK Level 2-16x3.0ML
- Database Sync Date
- 2026-08-09 09:29:18
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Platelet CHECK?
The registered manufacturer of record for Platelet CHECK is SYSMEX CORPORATION.
What is the Primary UDI-DI identifier for Platelet CHECK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CC118360.
What classification code is assigned to this device?
This device is registered under product classification code GJP.
Similar Classification Devices (GJP)
Other Devices by SYSMEX CORPORATION
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